US4315778A - Flux composition for ceramic color, containing no harmful heavy metal - Google Patents
Flux composition for ceramic color, containing no harmful heavy metal Download PDFInfo
- Publication number
- US4315778A US4315778A US06/137,956 US13795680A US4315778A US 4315778 A US4315778 A US 4315778A US 13795680 A US13795680 A US 13795680A US 4315778 A US4315778 A US 4315778A
- Authority
- US
- United States
- Prior art keywords
- weight
- flux
- lead
- ceramic color
- heavy metal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/062—Glass compositions containing silica with less than 40% silica by weight
- C03C3/064—Glass compositions containing silica with less than 40% silica by weight containing boron
- C03C3/066—Glass compositions containing silica with less than 40% silica by weight containing boron containing zinc
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
- C03C8/02—Frit compositions, i.e. in a powdered or comminuted form
- C03C8/06—Frit compositions, i.e. in a powdered or comminuted form containing halogen
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2205/00—Compositions applicable for the manufacture of vitreous enamels or glazes
Definitions
- This invention relates to fluxes for ceramic color which do not contain harmful heavy metal or metals.
- the present invention has been attained after earnest research works to obtain a flux composition in which such harmful heavy metals as lead, cadmium, barium, chromium or the like are not used.
- the baking temperature should be lower than the softening temperatures of vessels, i.e. they should be about 600° C. and should not be over 620° C. at the highest, their expansion coefficients should be close to those of glass vessels, they should have a good waterproofing characteristic, good alkali and acid resistance, and so on.
- the baking temperature should be lower than the softening temperatures of vessels, i.e. they should be about 600° C. and should not be over 620° C. at the highest, their expansion coefficients should be close to those of glass vessels, they should have a good waterproofing characteristic, good alkali and acid resistance, and so on.
- harmful metals mainly of lead, cadmium, barium, etc. among the components are contained.
- an objective material has been obtained by a composition consisting of 30 to 45% by weight of SiO 2 , 0 to 5% by weight of TiO 2 , 4 to 10% by weight of ZrO 2 , 13 to 18% by weight of B 2 O 3 , 18 to 23% by weight of ZnO, 0 to 3% by weight of CaO, 12 to 15% of the total of two or three kinds of R 2 O selected from Na 2 O, K 2 O and Li 2 O, 4 to 10% by weight of fluorine and 0 to 5% by weight of tin oxide.
- any of Na 2 O, K 2 O and Li 2 O of the R 2 O component does not exceed two third of the total amount of R 2 O components. Also when the total amount of Na 2 O, K 2 O and Li 2 O is greater than the amount of ZnO, where molar fraction of the R 2 O component>molar fraction of ZnO, the expansion coefficient increases and cracks are formed. If the amount of the ZnO component is 23% or more, the softening point is elevated. If the amount of the B 2 O 3 component is 13% or less in the flux, the softening point is also elevated, and when it is 18% or more, resistance to chemicals is deteriorated.
- CaO and TiO 2 components do not greatly influence the softening point of the expansion coefficient, and CaO has an effect of elevating the initial alkali resistance and TiO 2 has an effect of elevating initial acid resistance.
- the ZrO 2 is necessary for enhancing the resistance to chemicals. Tin oxide also is effective for enhancing the resistance to chemicals. Fluoride is necessary for lowering the softening point.
- the flux thus obtained was milled with an organic vehicle together with a heat-resistant inorganic pigment, and a paste-like or paint-like ceramic color is obtained.
- the organic vehicle used herein is one which gives good wetting to the flux and provides suitability of application.
- a typical such composition is from 10 to 30% by weight of at least one kind of a resin component such as rosin type resin, cellulose type resin, acrylic resin or the like dissolved in from 70 to 90% by weight of an organic solvent such as pine oil or the like. It is also possible to make the composition thermoplastic paste using a wax in place of an organic solvent such as pine oil or the like.
- the mixed raw materials were charged in a crucible made of a refractory material and heated and melted at a temperature of 1200° C.
- the melted materials were quenched by dropping in water to form small pieces in order to make the subsequent step of crushing easier.
- the quenched pieces were charged in a ball mill together with a suitable amount of water and finely divided, followed by dehydration and drying to obtain fine powder.
- the resulting paste ceramic colors were applied by screen printing on a commercially available soda-lime-silica glass using a 180 mesh screen and baked at a temperature of 560° ⁇ 620° C.
- the printed and baked glass plates were tested for alkali resistance and acid resistance under the condition of (A) and (B)
- the flux according to the present invention uses no lead the use of which has heretofore been considered as an indispensable condition for lower melting glasses, and further, it is possible to control the expansion coefficient and also impart water resistance, alkali resistance and acid resistance, such performances having been difficult to afford according to conventional lower melting lead-free fluxes. Moreover, since it does not contain any harmful heavy metal, there is no fear of environmental pollution and public nuisance.
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Glass Compositions (AREA)
- Surface Treatment Of Glass (AREA)
Abstract
A flux composition for ceramic color, containing no harmful heavy metal such as lead, cadmium, chromium, etc. is provided.
The flux composition consists mainly of 30 to 45% of SiO2, 0 to 5% of TiO2, 4 to 10% of ZrO2, 13 to 18% of B2 O3, 18 to 23% of ZnO, 0 to 3% of CaO, 12 to 15% of the total of two or three kinds of R2 O selected from Na2 O, K2 O and Li2 O, 4 to 10% of fluorine and 0 to 5% of tin oxide (% being all by weight).
The composition uses no lead which has been indispensable for lower melting glasses, and exhibits superior performances difficult to afford according to conventional lower melting lead-free fluxes.
Description
This invention relates to fluxes for ceramic color which do not contain harmful heavy metal or metals.
In the fluxes presently in use for ceramic color for the purpose of printing decorative designs, or trademarks, or indicating scales, etc. on glass vessels or the like, at least one harmful heavy metal such as lead, barium, cadmium or the like is usually used. These heavy metals may lead to the dangers of physical damage caused at the time of production and processing ceramic color, and the pollution of working environment, requiring a great deal of expenses for the equipments of waste disposal. Also, it causes apprehension among consumers that environmental pollution may occur.
With the above problems in mind, the present invention has been attained after earnest research works to obtain a flux composition in which such harmful heavy metals as lead, cadmium, barium, chromium or the like are not used.
To such ceramic color fluxes there are severe requirements of properties such that the baking temperature should be lower than the softening temperatures of vessels, i.e. they should be about 600° C. and should not be over 620° C. at the highest, their expansion coefficients should be close to those of glass vessels, they should have a good waterproofing characteristic, good alkali and acid resistance, and so on. On this account it has heretofore been impossible for commercially available products to satisfy these requirements unless harmful metals mainly of lead, cadmium, barium, etc. among the components are contained.
In the present invention a successful result has been attained by balancing the contents of alkali metals, an alkaline earth metal, and a zinc group element. Namely an objective material has been obtained by a composition consisting of 30 to 45% by weight of SiO2, 0 to 5% by weight of TiO2, 4 to 10% by weight of ZrO2, 13 to 18% by weight of B2 O3, 18 to 23% by weight of ZnO, 0 to 3% by weight of CaO, 12 to 15% of the total of two or three kinds of R2 O selected from Na2 O, K2 O and Li2 O, 4 to 10% by weight of fluorine and 0 to 5% by weight of tin oxide.
Among the above-mentioned compositions, it is preferable, in view of melting property of the flux, that any of Na2 O, K2 O and Li2 O of the R2 O component does not exceed two third of the total amount of R2 O components. Also when the total amount of Na2 O, K2 O and Li2 O is greater than the amount of ZnO, where molar fraction of the R2 O component>molar fraction of ZnO, the expansion coefficient increases and cracks are formed. If the amount of the ZnO component is 23% or more, the softening point is elevated. If the amount of the B2 O3 component is 13% or less in the flux, the softening point is also elevated, and when it is 18% or more, resistance to chemicals is deteriorated. Further, when the amounts of the CaO and TiO2 components are 3% or less, these components do not greatly influence the softening point of the expansion coefficient, and CaO has an effect of elevating the initial alkali resistance and TiO2 has an effect of elevating initial acid resistance. The ZrO2 is necessary for enhancing the resistance to chemicals. Tin oxide also is effective for enhancing the resistance to chemicals. Fluoride is necessary for lowering the softening point.
Mixed raw materials of oxides or salts which become oxides and a fluoride in the above-mentioned compositon are heated and melted at a temperature of 1100° C.˜1350° C. and then they are quenched, wet ground using a ball-mill or the like, dehydrated and dried to powder.
The flux thus obtained was milled with an organic vehicle together with a heat-resistant inorganic pigment, and a paste-like or paint-like ceramic color is obtained. The organic vehicle used herein is one which gives good wetting to the flux and provides suitability of application.
A typical such composition is from 10 to 30% by weight of at least one kind of a resin component such as rosin type resin, cellulose type resin, acrylic resin or the like dissolved in from 70 to 90% by weight of an organic solvent such as pine oil or the like. It is also possible to make the composition thermoplastic paste using a wax in place of an organic solvent such as pine oil or the like.
Following examples are to illustrate the composition of the present invention, and should not be construed as limiting the scope of the claim. All parts and % are by weight.
The following oxides, oxide-forming salts and fluoride are admixed
______________________________________
Component Parts by weight
______________________________________
Sodium Carbonate 7
Potassium Carbonate
6
Lithium Carbonate
10
Zinc Oxide 20
Calcium Carbonate
5
Boric Acid 30
Silicon Dioxide 35
Titanium Dioxide 3
Zirconium Silicate
5
Sodium Fluorosilicate
5
______________________________________
The mixed raw materials were charged in a crucible made of a refractory material and heated and melted at a temperature of 1200° C. The melted materials were quenched by dropping in water to form small pieces in order to make the subsequent step of crushing easier. Then the quenched pieces were charged in a ball mill together with a suitable amount of water and finely divided, followed by dehydration and drying to obtain fine powder.
Raw materials were mixed, melted and ground to a flux of fine powder as in Example 1 in the following ratio:
______________________________________
Component Parts by weight
______________________________________
Sodium Carbonate 10
Potassium Nitrate
6
Lithium Carbonate
8
Zinc Oxide 23
Calcium Carbonate
5
Boric Acid 25
Silicon Dioxide 35
Titanium Dioxide 3
Zirconium Silicate
10
Sodium Fluorosilicate
5
______________________________________
Following raw materials were mixed, melted and ground to a flux of fine powder as in Example I:
______________________________________
Component Parts by weight
______________________________________
Sodium Carbonate 4
Potassium Nitrate
9
Lithium Carbonate
7
Zinc Oxide 20
Calcium Carbonate
3
Boric Acid 25
Silicon Dioxide 29
Titanium Dioxide 4
Zirconium Silicate
13
Sodium Fluorosilicate
9
______________________________________
The fluxes obtained in Examples 1, 2 and 3 were compared with commercially available products.
For this purpose, to 900 g of the powder of the flux of Example 1 and 100 g of titanium white, an oil consisting of 75% by weight of pine oil, 20% by weight of rosin type resin, and 5% by weight of cellulose type resin, as an organic vehicle was added. After mixing in a muller mixer, the mixture was milled to form a paste like ceramic color. An organic vehicle was added to 900 g of the flux powder of Example II and 130 g of cobalt blue, and they were processed as in Example 1 to form a paste like ceramic color, and thus comparisons were carried out.
The resulting paste ceramic colors were applied by screen printing on a commercially available soda-lime-silica glass using a 180 mesh screen and baked at a temperature of 560°˜620° C. The printed and baked glass plates were tested for alkali resistance and acid resistance under the condition of (A) and (B)
(A) Alkali resistance test
______________________________________
NaOH 9% by weight
Test solution Na.sub.3 PO.sub.4 . 12H.sub.2 O
1% by weight
pure water 90% by weight
______________________________________
dipped at 88° C.±1° C. for 2 hours and 15 hours
(B) Acid resistance test
______________________________________
38% HCl 10% by volume
Test solution
pure water 90% by volume
______________________________________
dipped at 27° C.±5° C. for 10 minutes.
The results of the tests, and the presence or absence of cracks due to differences of the expansion coefficients are shown in the Table together with compositions of flux powder.
______________________________________
Com- Com-
Flux I Flux II Flux III mercial
mercial
of the of the of the flux con-
flux con-
present present present taining
taining
invention invention
invention
no lead
lead
______________________________________
SiO.sub.2 42 parts 35 parts
37 parts
31.9 parts
36.3 parts
TiO.sub.2 3 3 4 3 2.7
ZrO.sub.2 5 10 9 2.5
B.sub.2 O.sub.3
17 14 14 21.2 7.6
ZnO 20 23 20 16
CaO 3 3 2
CdO 3.5
PbO 39.0
BaO 20.6
Na.sub.2 O 4 6 6 8.8
K.sub.2 O 4 3 4 2.8
Li.sub.2 O 4 3 3 2.0
F 5 5 5 5.4 3.6
Baking
tempe- 600° C.
600° C.
600° C.
600° C.
600° C.
rature
(A)
test good good good bad good
(B)
test good good good bad good
Cracks none none none yes none
______________________________________
It is seen from the above-indicated results that the flux according to the present invention uses no lead the use of which has heretofore been considered as an indispensable condition for lower melting glasses, and further, it is possible to control the expansion coefficient and also impart water resistance, alkali resistance and acid resistance, such performances having been difficult to afford according to conventional lower melting lead-free fluxes. Moreover, since it does not contain any harmful heavy metal, there is no fear of environmental pollution and public nuisance.
Claims (1)
1. A flux composition for ceramic color containing no heavy metal and comprising 30 to 45% by weight of SiO2, 0 to 5% by weight of TiO2, 4 to 10% by weight of ZrO2, 13 to 18% by weight of B2 O3, 18 to 23% by weight of ZnO, 0 to 3% by weight of CaO, 12 to 15% by weight of the total of two or three kinds of R2 O selected from Na2 O, K2 O and Li2 O, 4 to 10% by weight of fluorine and 0 to 5% by weight of tin oxide.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8445079A JPS569246A (en) | 1979-07-05 | 1979-07-05 | Harmful heavy metal-free flux composition for glass coloring |
| JP54-84450 | 1979-07-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4315778A true US4315778A (en) | 1982-02-16 |
Family
ID=13830944
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/137,956 Expired - Lifetime US4315778A (en) | 1979-07-05 | 1980-04-07 | Flux composition for ceramic color, containing no harmful heavy metal |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US4315778A (en) |
| JP (1) | JPS569246A (en) |
| GB (1) | GB2053887B (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4493900A (en) * | 1982-02-08 | 1985-01-15 | Matsushita Electric Industrial Company, Limited | Low melting enamel frits |
| WO1990015782A1 (en) * | 1987-12-17 | 1990-12-27 | Ferro Corporation | Lead-free glass |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2068440A1 (en) * | 1991-07-01 | 1993-01-02 | Jaroslava M. Nigrin | Transparent lead-free and cadmium-free glazes |
| US6346493B1 (en) * | 1999-10-27 | 2002-02-12 | Ferro Corporation | Decorative glass enamels |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4160654A (en) * | 1977-10-25 | 1979-07-10 | Corning Glass Works | Method for making silver-containing glasses exhibiting thermoplastic properties and photosensitivity |
| US4179300A (en) * | 1977-01-27 | 1979-12-18 | Hoya Corporation | Optical glass |
| US4212919A (en) * | 1979-06-28 | 1980-07-15 | Corning Glass Works | Strengthened polychromatic glasses |
-
1979
- 1979-07-05 JP JP8445079A patent/JPS569246A/en active Pending
-
1980
- 1980-04-07 US US06/137,956 patent/US4315778A/en not_active Expired - Lifetime
- 1980-04-30 GB GB8014227A patent/GB2053887B/en not_active Expired
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4179300A (en) * | 1977-01-27 | 1979-12-18 | Hoya Corporation | Optical glass |
| US4160654A (en) * | 1977-10-25 | 1979-07-10 | Corning Glass Works | Method for making silver-containing glasses exhibiting thermoplastic properties and photosensitivity |
| US4212919A (en) * | 1979-06-28 | 1980-07-15 | Corning Glass Works | Strengthened polychromatic glasses |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4493900A (en) * | 1982-02-08 | 1985-01-15 | Matsushita Electric Industrial Company, Limited | Low melting enamel frits |
| WO1990015782A1 (en) * | 1987-12-17 | 1990-12-27 | Ferro Corporation | Lead-free glass |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS569246A (en) | 1981-01-30 |
| GB2053887B (en) | 1982-12-08 |
| GB2053887A (en) | 1981-02-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCF | Information on status: patent grant |
Free format text: PATENTED CASE |